Diazoacetylglycine

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Identification

Molecular formula
C4H6N4O3
CAS Number
119-42-6
IUPAC Name
2-amino-6-diazo-5-oxo-hexanoic acid
Molecular Weight
157.11g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4040g/cm3
Synonyms
6-Diazo-5-oxo-norleucine
Interesting facts

Exploring 2-amino-6-diazo-5-oxo-hexanoic acid

2-amino-6-diazo-5-oxo-hexanoic acid, often referred to in the scientific community for its intriguing molecular structure and biochemical significance, is a compound that showcases several fascinating properties.

Key Features:

  • Diazo Group: This compound features a diazo group (-N=N-), which is known for its reactivity and the role it plays in various chemical reactions, such as coupling reactions in organic synthesis.
  • Diverse Applications: Its structure and functional groups make it a candidate for applications in pharmaceuticals and biochemistry, particularly in the synthesis of novel compounds.
  • Biochemical Interest: The compound is related to amino acids, components critical for protein synthesis, and this connection has spurred research into its biological effects and potential medicinal uses.

Interesting Insights:

As a chemistry student or scientist, one might find it stimulating to examine how the presence of both amino and oxo groups can influence the reactivity of a compound. As noted by researchers, “the diazo functionality allows for versatile reactions, opening doors to innovative synthesis pathways.”

Furthermore, compounds like 2-amino-6-diazo-5-oxo-hexanoic acid demonstrate the intricate relationship between structure and reactivity in organic chemistry, making them subjects of ongoing research and inquiry. Studying such compounds enhances our understanding of both fundamental and applied chemistry.

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